Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00300 | A05 | 150663 | G | A | upstream_gene_variant | MODIFIER | c.-1117G>A| |
S208 S219 |
2 | BAA05g00300 | A05 | 150903 | G | A | upstream_gene_variant | MODIFIER | c.-877G>A| |
S129 |
3 | BAA05g00300 | A05 | 151908 | C | T | synonymous_variant | LOW | c.129C>T|p.Leu43Leu |
S146 |
4 | BAA05g00300 | A05 | 151915 | G | A | missense_variant | MODERATE | c.136G>A|p.Gly46Ser |
S116 |
5 | BAA05g00300 | A05 | 152307 | C | T | missense_variant | MODERATE | c.199C>T|p.Pro67Ser |
S208 S93 |
6 | BAA05g00300 | A05 | 152331 | C | T | missense_variant | MODERATE | c.223C>T|p.Arg75Cys |
S262 |
7 | BAA05g00300 | A05 | 152875 | C | T | synonymous_variant | LOW | c.564C>T|p.Leu188Leu |
S201 |
8 | BAA05g00300 | A05 | 153636 | C | T | missense_variant | MODERATE | c.820C>T|p.Leu274Phe |
S303 |
9 | BAA05g00300 | A05 | 153705 | C | T | missense_variant | MODERATE | c.889C>T|p.His297Tyr |
S136 |
10 | BAA05g00300 | A05 | 154167 | C | T | synonymous_variant | LOW | c.1032C>T|p.Cys344Cys |
S67 |
11 | BAA05g00300 | A05 | 154374 | G | A | missense_variant | MODERATE | c.1165G>A|p.Val389Met |
S206 S26 |
12 | BAA05g00300 | A05 | 155892 | C | T | missense_variant | MODERATE | c.2035C>T|p.Pro679Ser |
S181 |
13 | BAA05g00300 | A05 | 156079 | G | A | missense_variant | MODERATE | c.2131G>A|p.Ala711Thr |
S25 |
14 | BAA05g00300 | A05 | 156176 | C | T | missense_variant | MODERATE | c.2228C>T|p.Ser743Phe |
S274 |
15 | BAA05g00300 | A05 | 160852 | G | A | downstream_gene_variant | MODIFIER | c.*3714G>A| |
S34 |